Katie Coleman: There would be no “my story”, without “our story”
Katie Coleman shared a post on X:
“This month my husband and I celebrate our 4th anniversary. We eloped in Oct 2020 after we decided even though we’d barely known each other for over a year, we didn’t want to wait until we could plan a big wedding to begin our forever.
I would be diagnosed with stage IV cancer, just two months later. I have to say, my favorite part of reactions to my memoir so far has been sharing our love story.
It brings a smile to my face every time someone new starts reading it, they almost all comment about or ask about him. Today marks exactly one month until the release of my memoir. There would be no my story, without our story.”
Katie Coleman, Product and Engineering Lead at the Rare Cancer Research Foundation and President of the Chromophobe and Oncocytic Tumor Alliance (COA), is a dedicated software engineer with a mission for creating intuitive, user-friendly products. As a rare kidney cancer survivor, she is deeply committed to medical research and advocacy. Her personal experience helps her to promote collaborations that advance rare cancer research. Katie combines her technical expertise and unique perspective to develop products that improve patient outcomes and support the foundation’s mission.
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